THE PHILIPS MP20,MP30,MP40,MP50,MP60,MP70,MP80 AND MP90 INTELLIVUE ATIENT MONITORS

Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)

PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH

The following data is part of a premarket notification filed by Philips Medizinsysteme Boblingen Gmbh with the FDA for The Philips Mp20,mp30,mp40,mp50,mp60,mp70,mp80 And Mp90 Intellivue Atient Monitors.

Pre-market Notification Details

Device IDK060541
510k NumberK060541
Device Name:THE PHILIPS MP20,MP30,MP40,MP50,MP60,MP70,MP80 AND MP90 INTELLIVUE ATIENT MONITORS
ClassificationMonitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)
Applicant PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH HEWLETT PACKARD STR. 2 Boblingen,  DE D 71034
ContactHerbert Van Dyk
CorrespondentHerbert Van Dyk
PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH HEWLETT PACKARD STR. 2 Boblingen,  DE D 71034
Product CodeMHX  
Subsequent Product CodeBZQ
Subsequent Product CodeCBQ
Subsequent Product CodeCBR
Subsequent Product CodeCBS
Subsequent Product CodeCCK
Subsequent Product CodeCCL
Subsequent Product CodeNHO
Subsequent Product CodeNHP
Subsequent Product CodeNHQ
CFR Regulation Number870.1025 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-03-01
Decision Date2006-03-24
Summary:summary

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